An inherited metabolic disease that is has its basis in the disruption of glutathione metabolic process.
Comprehensive, easy-to-understand information about this condition
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gamma-glutamylcysteine synthetase deficiency
MONDO:0009259
gamma-glutamyl transpeptidase deficiency
MONDO:0009285
spondylometaphyseal dysplasia, Sedaghatian type
MONDO:0009593
5-oxoprolinase deficiency
MONDO:0009825
inherited glutathione synthetase deficiency
MONDO:0017909
inherited lipoic acid biosynthesis defect
MONDO:0018424